# K091060: Vesocclude Ligating Clip

- Pathway: 510(k) (Traditional)
- Applicant: Vesocclude Medical, LLC
- Decided: Sep 23, 2009 after 162 days
- Product code: FZP (Clip, Implantable)
- Device class: 2
- Regulation: 21 CFR 878.4300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K841547 (1984). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K901303: Horizon Surgical Ligating and Marking Clip, Horizon Surgical, Inc. (1990) Summary page 1.
- K982313: Horizon Titanium Clips, Horizon Tantalum Clips, Weck Closure Systems (1998) Summary page 1.
- K841547: Hemoclip Ligating Clips Med/SML, Edward Weck, Inc. (1984) Summary page 1.
- K841548: Hemoclip Ligating Clips M/Large, Edward Weck, Inc. (1984) Summary page 1.
- K841549: Hemoclip Automatic Clips Medium, Edward Weck, Inc. (1984) Summary page 1.

## Cited in the summary but kept off the family tree
- K861992: Model 43200A Cardiac Monitor, Hewlett-Packard Co. (1986). Our reading of the summary gave K861992, FDA’s number for Model 43200A Cardiac Monitor (Hewlett-Packard Co.). Its FDA name has none of the distinctive words the summary uses for the device it names, “Teleflex Medical Atrauclip Ligating Clips”. Kept off the family tree. Summary page 1.

## Indications for use
Vesocclude ligating clips are intended for use in procedures involving vessels or anatomic structures for which the user determines ligating clips are the best choice. Users should select the size and amount of the clips based on upon their experience, judgment, and needs.

Source page: https://510kreport.com/device/K091060
Methodology: https://510kreport.com/methodology